Evidence map›Paper›PMID 30291873›Full record

ReviewPharmacological research2018

Neuronal and astrocytic primary cilia in the mature brain.

Ashley Sterpka, Xuanmao Chen

Open access · greenAbstract readReview
In one paragraph

Review in Pharmacological research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
5.6field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

60 citing papers in PubMed, 85 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Primary cilia and neural computation.Journal of biomedical science · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. PathogenicLife science alliance · 2025
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Ashley SterpkaDepartment of Molecular, Cellular and Biomedical Sciences, University of New Hampshire, Durham, NH, 03824, United States.
Xuanmao ChenDepartment of Molecular, Cellular and Biomedical Sciences, University of New Hampshire, Durham, NH, 03824, United States. Electronic address: Xuanmao.Chen@unh.edu.
University of New Hampshire · US

Funding

TLR-TRIF mediated induction of GLI3 modulates innate inflammatory responsesP20GM113131 · NIGMS · UNIVERSITY OF NEW HAMPSHIRE · PI DON Michael WOJCHOWSKI · 2017 to 2026
$22.8M
The role of AC3 in neuronal activity and depression-related phenotypeR21MH105746 · NIMH · UNIVERSITY OF WASHINGTON · PI CHEN, XUANMAO · 2015 to 2016
$398k
Type 3 Adenylyl Cyclase in Neuronal Primary Cilia and its Roles in Brain AgingK01AG054729 · NIA · UNIVERSITY OF NEW HAMPSHIRE · PI CHEN, XUANMAO · 2017 to 2017
$126k
NIA NIH HHS K01 AG054729NIGMS NIH HHS P20 GM113131NIMH NIH HHS R21 MH105746
6 · The paper itself

Abstract

Primary cilia are tiny microtubule-based signaling devices that regulate a variety of physiological functions, including metabolism and cell division. Defects in primary cilia lead to a myriad of diseases in humans such as obesity and cancers. In the mature brain, both neurons and astrocytes contain a single primary cilium. Although neuronal primary cilia are not directly involved in synaptic communication, their pathophysiological impacts on obesity and mental disorders are well recognized. In contrast, research on astrocytic primary cilia lags far behind. Currently, little is known about their functions and molecular pathways in the mature brain. Unlike neurons, postnatal astrocytes retain the capacity of cell division and can become reactive and proliferate in response to various brain insults such as epilepsy, ischemia, traumatic brain injury, and neurodegenerative β-amyloid plaques. Since primary cilia derive from the mother centrioles, astrocyte proliferation must occur in coordination with the dismantling and ciliogenesis of astrocyte cilia. In this regard, the functions, signal pathways, and structural dynamics of neuronal and astrocytic primary cilia are fundamentally different. Here we discuss and compare the current understanding of neuronal and astrocytic primary cilia.

Indexed as

Abnormalities, MultipleAdenylyl CyclasesADP-Ribosylation FactorsAnimalsAstrocytesBrainCiliaHumansMental DisordersNeuronsObesityadenylate cyclase 3Adenylyl CyclasesADP-Ribosylation FactorsARL13B protein, humanARL13BAstrocytesPrimary ciliaSonic HedgehogType 3 adenylyl cyclase (AC3)

Identifiers

PMID30291873
PMCPMC6410375
OpenAlexW2895663716

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.